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. 2015 Oct 16;53(11):3430–3437. doi: 10.1128/JCM.01714-15

TABLE 2.

SNP detection probes of the 23S rRNA rrl gene 2058A-to-G or -C and 2059A-to-G mutation and the erm(41) gene 28T-to-C mutation

Probe Gene Nucleotide position(s) Base change LNA probe sequencea Tm (°C)
WT_MAB 23S rRNA 2058–2059 AA to AA 5′-HEX-ACG+A+A+A+AGA+C+CC-IABkFQ-3′ 65.1
AA_2058G 23S rRNA 2058 AA to GA 5′-Cy5-ACG+A+G+A+AGA+CCC-IABkFQ-3′ 68.2
AA_2058C 23S rRNA 2058 AA to CA 5′-6FAM-ACG+A+C+A+AGA+CCC-IABkFQ-3′ 66.8
AA_2059G 23S rRNA 2059 AA to AG 5′-6FAM-ACG+A+A+G+AGA+CCC-IABkFQ-3′ 68.2
C Allele erm(41) 28 T to C 5′-6FAM-CCA+G+C+GGGGC/IABkFQ-3′ 67.4
T Allele erm(41) 28 T to T 5′-HEX-CCA+G+T+GGGGC-IABkFQ-3′ 69.3
a

HEX, hexachlorofluorescein; 6FAM, 6-carboxyfluorescein; IABkFQ, Iowa Black fluorescent quencher.